UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
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SCHEDULE 14A
INFORMATION
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November 21, 2022
Dear Fellow Actinium Shareholder:
It is with great enthusiasm that we share the tremendous progress
we have made in 2022. The success of our Iomab-B pivotal trial, the strong overall survival data
from our earlier stage Actimab-A+CLAG-M trial and
exciting pre-clinical data from our
R&D collaborations, have laid a strong foundation for a bright
future for the company. We believe the clinical data sets for
Iomab-B and Actimab-A, which we expect to share in more detail by
year-end, are the harbinger of a
potential paradigm change in the treatment of relapsed/refractory
AML (r/r AML), an area of high unmet need, as these patients have a
very poor survival prognosis. We have also made significant strides
in building our leadership team with key recent hires in core
functional areas in anticipation of these key milestones and they
are energized by this data and the opportunity to realize its full
potential.
Investment dollars keep pouring into our niche radiotherapy sector.
While the number of companies is growing, the majority feature
undifferentiated, nascent, or at best very early-stage clinical programs. Actinium is truly
differentiated by our clinical focus on late-stage, hematological malignancies, a growing
number of earlier programs in solid tumors, a well-established supply chain into major oncology
centers of excellence, and an industry leading intellectual
property portfolio. We are at an inflection point in the Company’s
history with the opportunity to establish ourselves as a leader in
the radiotherapeutics industry and are excited to provide you with
this update on our Iomab-B and
Actimab-A clinical programs, R&D,
partnerships, and overall organizational development.
We were thrilled to announce highly positive topline results from
the pivotal Phase 3 SIERRA trial for our lead asset
Iomab-B last week. The SIERRA trial
met its primary endpoint of durable Complete Remission (dCR) of
6 months post-initial remission
after a bone marrow transplant (BMT) with high statistical
significance (p<0.0001) compared to the control arm. The trial
was conducted in patients 55 years of age or older with r/r
AML who typically cannot access a potentially lifesaving BMT as
they are deemed unfit and thus unable to tolerate standard
chemotherapy-based conditioning. Trial
results showed that with Iomab-B
conditioning, these patients have increased access to a BMT with a
clinically meaningful duration of complete remission, along with a
favorable safety profile, potentially establishing a new treatment
option for the majority of the 10,000 r/r AML patients in the
U.S. who are deemed unfit for BMT with current approaches.
Driven by strong encouragement from SIERRA trial investigators who
represent the leading transplant physicians at the largest volume
transplant hospitals, we expect to present detailed SIERRA trial
data at upcoming BMT focused medical conference(s). We look forward
to unveiling this data in a setting that will maximize the impact
of our trial results for our target audience of transplant
physicians as our team works assiduously toward a Biologics License
Application (BLA) filing and Early Access Program in 2023.
We strongly believe that based on these results and prior clinical
data in over 12 trials and several hundred patients in other blood
cancers, Iomab-B has the potential to
establish a new standard of care and to increase access to BMT with
improved patient outcomes not only in AML but in MDS, ALL,
Hodgkin’s and Non-Hodgkin’s Lymphoma
and Multiple Myeloma. These results from our well-controlled SIERRA trial will help drive
development of the broader opportunity for the Iomab-B clinical program that includes label expansion
and also for Iomab-ACT, a low dose
version of the Iomab-B construct that
is focused on lymphodepletion and reduced intensity conditioning
prior to CAR-T and gene and cellular
therapies. We look forward to sharing additional details on our
Iomab-B expansion strategy and sharing
more on our Iomab-ACT trial with
Memorial Sloan Kettering and the broader development program next
year.
We are also excited to report results from our industry leading
Actinium-225 based radiotherapeutic
program Actimab-A which has been
tested in six trials and ~150 AML patients demonstrating high
response rates and good tolerability as a single agent.
Actimab-A is being developed in
combination with other regimens to exploit mechanistic synergies
with the objective of establishing it as a backbone therapy. The
Actimab-A + CLAG-M Phase 1 trial was conducted in
high-risk, r/r AML patients who had
failed two or more lines of therapy, many of whom had TP53
mutations or have failed venetoclax, and consequently have dismal
survival of approximately two months. Previously reported data
showed an Overall Response Rate of 67%, 83% at the recommended
Phase 2 dose, high rates of MRD negativity or undetectable
AML, and a clear improvement in survival for this difficult to
treat patient population.
We are elated to update these results and report a meaningful
improvement in median Overall Survival of 53% and 32% at one and
two years. These survival outcomes are exciting as they are as
much as double the one- and two-year
survival rates r/r AML patients can expect with current therapies.
We are enthused by this compelling proof of
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concept data as it validates our strategy of developing
Actimab-A as a backbone therapy and
sets the foundation for advanced development. The full data set
will be presented at the annual meeting of the American Society of
Hematology in December, and we will provide a program update on
future development in 2023.
R&D at Actinium is robust, differentiated and practical and
given the competitive environment, we are glad that we made the
strategic decision years ago to avoid programs with low
competitive differentiation potential where multiple radiotherapy
companies are focused. Our research collaborations with
Astellas, AVEO Oncology and EpicentRx establish our work with
immunotherapies and in solid tumors. Our R&D team has ably
supported advancement of our Iomab-B
and Actimab-A programs in hematology.
The Iomab-ACT and Actimab-A combination strategy programs have been
informed by their efforts. Solid tumor programs with partner
Astellas and the HER3 targeted radiotherapy are novel and cutting
edge, as is our work with daratumumab-Ac-225 and other
radiotherapy combinations with the immunotherapy
magrolimab-CD47 checkpoint inhibitor in both liquid and solid
tumors. Underpinning these programs is our expanded patent
portfolio of over 195 issued patents and pending patent
applications worldwide. Our IP includes several patent families to
manufacture Actinium-225 in a
cyclotron, and valuable know-how. When
appropriate, we are well-positioned to
leverage this technology to produce Actinium-225. We look forward to sharing updates as these
programs advance to the next phase.
Our balance sheet is strong with the $111.8 million cash
reported at the end of 3Q:2022 expected to fund us well into 2025
and enable us to achieve several more value creating milestones.
Our partnership with Immedica Pharma AB to commercialize
Iomab-B in the EUMENA region provided
a $35 million payment upfront and has the potential for up to
$452 million in milestone payments and mid-twenty percent royalties. The market potential is
extremely compelling in the EU and approximately 50% larger with
15,000 patients with r/r AML and double the number of BMTs
performed than in the US.
Our achievements this year provide a stellar foundation upon which
we can execute on our corporate strategy as we continue the
momentum into 2023. We are hyper focused on delivering a successful
BLA filing to obtain approval for Iomab-B and building the capabilities for a successful
commercial launch. We will continue to advance our clinical
programs by focusing on the Iomab-B
lifecycle management plan, Actimab-A
combination trials and Iomab-ACT
program in cell and gene therapies. We will continue to advance our
R&D programs and partnerships into the next phases of
development.
We have continued to bolster our leadership team this year to
execute and deliver on our strategic plan. Despite the competitive
hiring market in the industry, we have continued to attract key
talent, including senior leaders across the clinical, commercial,
manufacturing, and G&A functions. Additional details on the
profiles of our expanded team are included in the Appendix. We will
need to continue to hire great talent and in order to attract such
individuals to drive value creation, we request that you support
the options plan proposal recommended by your Board of Directors in
the proxy statement. We ask for your much-needed support, which will enable us to deliver
value to you, our shareholders.
As we race toward a very eventful end of year, we are energized to
forge forward with the same intensity to prepare for a monumental
year for the company in 2023. Your continued support has made this
year possible, and TEAM Actinium thanks you for your unwavering
support to helping us achieve our goal to bring innovative
medicines to people who urgently need new treatment options.
Sincerely and on Behalf of TEAM ACTINIUM,

Sandesh Seth
Chairman and Chief Executive Officer
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Appendix — Review
and Outlook
In this section, we share our vision for building a leading
specialty radiotherapeutics company, following a pivotal (pun
intended) year for the Company with positive Phase 3 SIERRA
trial results that could establish a new treatment paradigm for the
difficult-to-treat r/r AML population. Iomab-B has the potential to greatly improve the
patient journey and the way patients are being managed to provide
them greater access to BMTs. Additional label enhancing and life
cycle management studies are needed to further develop
Iomab-B to establish it as a universal
conditioning agent for various hematological malignancies. The
compelling data from the Actimab-A +
CLAG-M combination trial validates our
strategy of developing Actimab-A as a
backbone therapy in AML and other hematological malignancies, and
we look forward to a comprehensive update on this program next
year. Recent additions to our senior leadership team positions us
well to execute seamlessly in the coming year, with details
highlighted in their biographies.
The
Transformational Opportunity for Targeted Conditioning
Remissions in the r/r AML population are difficult to achieve.
Preparation of the bone marrow for transplant requires conditioning
with either high dose or reduced intensity chemotherapy and/or
external radiation. Patients are often unable to achieve a
remission or are not medically fit to tolerate current conditioning
regimens — their prognosis is poor. This results in
disease relapse or limited access to BMT, the only curative
treatment option for the r/r AML population. Iomab-B represents a potential paradigm shift as
patients with active disease can be effectively conditioned and
access BMT with universal engraftment.
Of the nearly 21,000 patients diagnosed with AML each year, ~50% of
patients will become relapsed or refractory, yet less than 500 r/r
AML or just 4.5% of patients received a BMT. Typically, r/r
AML patients are not transplanted as they are unfit and cannot
withstand highly toxic chemotherapy-based conditioning regimens to myeloablate their
bone marrow before receiving the hematopoietic stem cells. With
survival of two to four months expected for this population
without a potentially lifesaving BMT, our focus is on increasing
patient access to a BMT and improving their outcomes via
Iomab-B, which is well tolerated due
to its highly targeted nature. We believe that Iomab-B can address this initial market of ~10,000 r/r
AML patients who do not have access to potentially curative BMT
with existing treatment approaches.
The recently announced topline results from the SIERRA (Study of
Iomab-B in Elderly Relapsed or
Refractory AML) trial showed that Iomab-B met the primary endpoint of durable complete
remission (dCR) of 6-months following
initial complete remission after HCT with a high degree of
significance (p<0.0001) compared to the control arm. The SIERRA
trial is a randomized, multi-center,
controlled study which compared Iomab-B as a conditioning regimen prior to a BMT versus
a control arm which allowed all current means of conventional care
with the intent to transplant these patients. Iomab-B improved BMT access, and produced a
statistically higher number of durable remissions, a major clinical
benefit, in patients not considered eligible for BMT.

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The positive Iomab-B Phase 3
SIERRA trial results support continued expansion of targeted
conditioning for BMT in other blood cancers, cellular therapy and
gene therapy indications. We plan to leverage this clinical data,
alongside our prior clinical experience in multiple r/r
hematological malignancies to disrupt today’s conditioning
regimens, with a potential game-changer that can improve access and outcomes for
hard-to-treat patients who have no options. We believe
leveraging our experience developing Iomab-B and prior clinical data to expand our
conditioning program into cell and gene therapy indications, an
evolving and high-growth area of
treatment innovation, can significantly expand the number of
patients who could benefit from Iomab-B or Iomab-ACT. We intend to continue to develop the
Iomab-ACT program as a low-dose version of Iomab-B designed specifically for use prior to
CAR-T and gene therapies, ultimately
with the same value proposition as Iomab-B — to improve overall access and
outcomes for patients who need cellular or gene therapies.
With the highly positive topline data in hand and strong
investigator support, we look forward to highlighting additional
SIERRA data at upcoming BMT focused conferences to convey
Iomab-B’s value proposition to our
target physician community. Our team is hard at work and focused on
submitting a BLA in 2023, with the intent of securing what we hope
will be the first of many approved indications for
Iomab-B. We are also progressing our
efforts to initiate an Early Access Program that will broaden the
real-world experience with
Iomab-B. In 2023, we are excited
to build upon the promise of Iomab-B
by further developing the lifecycle plan and continue to make
progress on Iomab-ACT.
Discovering High Potential
of Actimab-A in
r/r AML
Our Actimab-A program demonstrates our
leadership in the clinical development of Ac-225 therapeutics, as we focus this industry
leading alpha-isotope based
radiotherapy program as a backbone therapy for novel combinations
in r/r AML. Actimab-A is the
first radiotherapeutic for r/r AML and has the unique value
proposition of broad applicability, a differentiated mechanism of
action, and targeted precision that is well-tolerated with minimal toxicity. Specifically,
Actimab-A targets CD33, which is
expressed in virtually all AML patients regardless of cytogenetics
or mutations and enables potent alpha radiation to be directed
against radiosensitive AML cells that have no known resistance or
repair mechanism when hit with the Ac-225 isotope payload that causes double stranded
breaks in DNA.
We believe that Actimab-A in
combination with chemotherapy, targeted agents or immunotherapy, in
r/r AML as a backbone therapy, represents a significant opportunity
to improve patient outcomes in AML based on the data being
generated thus far. We have demonstrated preclinically that
combinations of Actimab-A and
venetoclax, a BCL-2 inhibitor, have
mechanistic synergies. Overexpression of MCL-1, an anti-apoptotic
protein, is associated with resistance to venetoclax in
AML. Actimab-A kills tumors cells
with DNA double-strand breaks and
downregulates MCL-1, which can
(re-)sensitize AML cells or reduce tumor resistance to venetoclax.
In our ongoing clinical trial with Actimab-A and venetoclax, we are exploring the optimal
dose of Actimab-A, as well as the
dosing regimen of the combination. The more advanced
Actimab-A + CLAG-M clinical trial has yielded data that
demonstrate favorable outcomes with improved survival when
Actimab-A is combined with this
intensive chemotherapy regimen. The scientific rational for this
combination is to use sequential administration of CLAG-M, a powerful chemotherapy regimen, followed by
Actimab-A for its precision targeting
ability that produces double-strand-DNA breaks
that lead to cancer cell death to mop up residual disease.
We are advancing Actimab-A in
combination with CLAG-M in a
phase I/II study, which has produced strong results in fit r/r
AML patients. The data suggest a manageable safety profile and
promising response rates. The study, enrolled patients with
multiple prior treatments (Median 2 lines of prior therapy (range:
1 – 5)), including prior BMT and Venetoclax. The patient
population represented a subset of patients who are extremely
difficult to treat and have very poor outcomes on available
therapies. Patients were a median age of 63 years and 57% had
adverse cytogenetics with 52% having TP53 mutations. 55% of
patients had failed prior BMT, 55% received prior Venetoclax
therapy and 52% had secondary AML. As we reported earlier, the
trial showed an Overall Response Rate (ORR) of 67% from all dose
cohorts including subtherapeutic doses of Actimab-A and an 83% ORR at the recommended Phase 2
dose. Importantly, MRD negativity, which indicates a deep remission
with no detectable disease, was 72% with Actimab-A + CLAG-M.
To provide context for this analysis, the median OS in patients who
relapse post venetoclax is less than 3 months and the median OS in
patients who relapse with a TP53 mutation is less than 2
months.
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We recently announced that Overall Survival (OS) data from the
Actimab-A + CLAG-M combination trial has been accepted for oral
presentation at the American Society of Hematology (ASH) Annual
Meeting & Symposium in December. The ASH abstract reported
a 12-month median OS among all
patients, and a 1-year OS of 53% and
2-year OS of 32%, which are as much as
double or more what can be expected with available therapies in
this setting. Overall survival has been dismal in r/r AML patients,
especially those who have adverse cytogenetics or failed venetoclax
based treatment. These results are highly encouraging and show that
the high rates of responses and MRD negativity are translating to a
meaningful survival benefit as can be evidenced in the figure
below.
Improved Survival Outcomes with Actimab-A + CLAG-M

Overall survival reported
in abstract accepted for oral
presentation at ASH adapted
to include results in comparable patients from other
studies
The complete data will be presented at ASH, and we look forward to
sharing more on our plans for advanced development of this very
promising treatment regimen next year.
Further Bolstering of Our
Senior Leadership Team
Our people make the foundation to our success, and we are extremely
proud that we continue to attract top talent to Actinium as we
effectively navigate the challenges in the talent market. We are
delighted to have welcomed the following key additions to our team
in anticipation of expected positive news we have now received on
both Iomab-B and Actimab-B as they will significantly enhance our ability
to execute our corporate plan across key functions:
Leadership
Position
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Relevant Qualifications and
Recent Accomplishments
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Caroline Yarbrough
Chief Commercial Officer
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• Portfolio
General Manager US Oncology at Novartis Innovative Medicines with
full P&L responsibility for a $1.5BN revenue group of oncology
brands and development assets
• Led
the commercial team that successfully launched SCEMBLIX in
CML. Led strategic account management during the launch of
KYMRIAH, the first approved CAR-T
product
• Held
leadership roles in both Global and US businesses, across Oncology
and specialty medicines at companies including GSK, BMS, Viropharma
and Merck
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Leadership
Position
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Relevant Qualifications and
Recent Accomplishments
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Jenny Hsieh
Chief Strategy Officer
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• Nearly
two decades of experience in leading and developing corporate
strategies across the healthcare and life sciences industries
• Led
Corporate Strategy at Immunomedics to help transform the
clinical-stage company into a
commercial organization (acquired by Gilead for $21BN following the
FDA approval of Trodelvy® in
triple-negative breast cancer)
• Advised
payers, providers, and life sciences companies as a management
consultant at several firms
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Sunitha
Lakshminarayanan
SVP, CMC and Product Development
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• 20+ years
of experience and technical expertise across biologics,
biosimilars, vaccines and cell/gene therapy products. Previously
responsible for global licensure of two autologous cell therapies,
Breyanzi® and
Abecma® as Executive
Director, Global Process Engineering at BMS for Cell Therapy
• Led
several BLA fillings, including approvals for Breyanzi®, Abecma®, Releuko® and
Fylnetra®
• Responsible
for new cell therapy facility build-outs for network expansions, technology
transfers, product life-cycle
management, new technology commercialization, comparability, and
Global MS&T labs
• Held
leadership roles at Kashiv BioSciences, Progenics, Laureate Pharma
and BioReliance
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Akash Nahar, MD
VP, Clinical Development
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• Over
15 years of hematology-oncology
research and development experience in academia and industry
• Held
positions of increasing responsibilities, most recently serving as
Global Product Development Lead for hematology programs at Merck,
leading a team of physicians responsible for the development of the
Keytruda® in Hodgkin’s
lymphoma, and other developmental products for hematological
malignancies, in addition to successfully filing two sBLA for
Keytruda®
• Board-certified
in pediatrics, hematology/oncology, and oncology. Faculty member at
St. Christopher’s Hospital for Children in Philadelphia and an
Associate Professor in pediatrics at Drexel University
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Madhuri Vusirikala,
MD
VP, Clinical Development,
Bone Marrow Transplant and Cellular Therapies
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• Accomplished
bone marrow transplant physician and hematologist with over
20 years of clinical experience and board-certified in internal medicine, hematology and
oncology
• Professor
of Internal Medicine in the Division of Hematology/Oncology and
Medical Director of the Adult Allogeneic BMT Program at UT
Southwestern Medical Center in Dallas. Primary investigator for
most clinical trials at UT Southwestern related to BMT
• Member
on the NCCN panels for Hematopoietic Cell Transplantation and Acute
Lymphoblastic Leukemia committees
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Leadership
Position
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Relevant Qualifications and
Recent Accomplishments
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Patrik Brodin, MSc,
PhD
VP, Radiation Sciences
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• Board-certified
Medical Physicist & American Board of Radiology
Therapeutic Medical Physics Diplomat. Previously Assistant
Professor/Senior Physicist at Montefiore/Einstein (Radiation
Oncology)
• Spearheaded
development of new approaches in radiation-driven immunotherapy and solutions to reduce risk
of severe treatment complications associated with high-dose radiation therapy
• Authored
over 60 peer-reviewed publications and
presented at national and international meetings including oral
presentations at ESTRO, ASTRO, AAPM and PTCOG
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Steve Dressel
VP, Strategic Finance and Analysis
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• Nearly
20 years of corporate finance and commercial experience
• Previously,
was the Senior Director, FP&A at Dewpoint Therapeutics
responsible for budgeting, long-term
planning, and analyses
• Held
finance leadership roles at Akebia Therapeutics that developed and
marketed Auryxia®, and spent
10 years at Regeneron in finance roles with increasing
responsibility supporting Praulent and EYLEA
• Began
career at Bio-IB, a life science
focused investment bank
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Elaina Haeuber
VP, Head of Clinical Operations
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• Over
20 years of clinical research operations and project
management experience
• Previously,
the Vice President, Operations at WCG, overseeing data safety
monitoring boards and independent event adjudication for clinical
studies
• As
Executive Director, Operations Management at Syneos Health, led
regional and global project and clinical management teams of up to
300 staff for oncology and hematology trials
• Supported
programs in including Tecentriq for multiple indications, Zynteglo,
the first cell-based gene therapy
approved for beta-thalassemia, and
Skysona, a gene therapy for early, active cerebral ALD
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More about the company is available on our web site www.actiniumpharam.com
in general and with investor related materials accessible at
https://ir.actiniumpharma.com.
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November 21, 2022
Dear Fellow Stockholders:
You are cordially invited to attend the Annual Meeting of
Stockholders (the “Annual Meeting”) of Actinium Pharmaceuticals,
Inc. to be held at 9:30 a.m., Eastern Time, on
December 8, 2022, at The Garden City Hotel, 45 Seventh
St, Garden City, NY 11530.
Annual Meeting
Details
Enclosed with this letter are your Notice of Annual Meeting of
Stockholders (the “Notice of Annual Meeting”), proxy statement and
proxy card. Also provided is the Company’s 2021 Annual Report,
which includes our annual report on
Form 10-K for the fiscal
year ended December 31, 2021. The proxy statement describes
the business that will be acted upon at the Annual Meeting.
Accordingly, we urge you to review the accompanying material
carefully and to promptly return the enclosed proxy card or voting
instruction form. Our proxy statement and the 2021 Annual Report
are also available at www.viewproxy.com/actiniumpharma/2022.
While as of the date of this proxy statement we are intending to
hold the Annual Meeting in a physical format, as part of our
precautions regarding the coronavirus, or COVID-19, we reserve the right to reconsider the date,
time, and/or means of convening the Annual Meeting, including
holding the Annual Meeting by means of remote communications. If we
take this step, we will announce the decision to do so as soon as
practicable via a press release that will also be filed with the
Securities and Exchange Commission (the “SEC”) as proxy material,
as well as by posting details on our website at https://www.actiniumpharma.com/. Please
monitor our press releases and check our website regularly until
the Annual Meeting for updated information.
You are required to register in advance of the Annual Meeting if
you plan to attend the Annual Meeting in person. If you wish to
register in advance of the Annual Meeting, please contact our
investor relations office by no later than November 28, 2022,
by e-mail to
investorrelations@actiniumpharma.com, mail to Actinium
Pharmaceuticals, Inc., 275 Madison Avenue, 7th Floor,
New York, New York 10016, or telephone at
(646) 677-3875.
Your vote is very important, regardless of the number of shares of
our voting securities that you own. Whether or not you expect to be
present at the Annual Meeting, after receiving the Notice of Annual
Meeting please vote as promptly as possible to ensure your
representation and the presence of a quorum at the Annual Meeting.
As an alternative to voting in person at the Annual Meeting, you
may vote via the Internet, by telephone, or by signing, dating and
returning the proxy card that is enclosed with the Notice of Annual
Meeting. If your shares are held in the name of a broker, trust,
bank or other nominee, and you receive these materials through your
broker or through another intermediary, please complete and return
the materials in accordance with the instructions provided to you
by such broker or other intermediary or contact your broker
directly in order to obtain a proxy issued to you by your nominee
holder to attend the Annual Meeting and vote in person at the
Annual Meeting. Failure to do so may result in your shares not
being eligible to be voted by proxy at the Annual Meeting. On
behalf of the Board of Directors, I urge you to submit
your vote as soon as possible, even if you currently plan to attend
the meeting in person.
On behalf of the team at Actinium,
Sincerely,
/s/ Sandesh Seth
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Sandesh Seth
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Chairman and Chief Executive Officer
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ACTINIUM PHARMACEUTICALS,
INC.
275 Madison Avenue,
7th
Floor
New York, New York 10016
NOTICE OF ANNUAL MEETING OF STOCKHOLDERS
To Our Stockholders:
NOTICE IS HEREBY GIVEN that the 2022 Annual Meeting of Stockholders
(the “Annual Meeting”) of Actinium Pharmaceuticals, Inc. (the
“Company”) will be held on Thursday, December 8, 2022, at
9:30 a.m. (Eastern Time) at The Garden City Hotel, 45 Seventh
St, Garden City, NY 11530. You are required to register in
advance of the Annual Meeting if you plan to attend the Annual
Meeting in person. If you wish to register in advance of the Annual
Meeting, please contact our investor relations office by no later
than November 28, 2022, by e-mail
to investorrelations@actiniumpharma.com, mail to Actinium
Pharmaceuticals, Inc., 275 Madison Avenue, 7th Floor,
New York, New York 10016, or telephone at
(646) 677-3875.
While as of the date of this proxy statement we are intending to
hold the Annual Meeting in a physical format, as part of our
precautions regarding the coronavirus, or COVID-19, we reserve the right to reconsider the date,
time, and/or means of convening the Annual Meeting, including
holding the Annual Meeting by means of remote communications. If we
take this step, we will announce the decision to do so as soon as
practicable via a press release that will also be filed with the
SEC as proxy material, as well as by posting details on our website
at https://www.actiniumpharma.com/. Please
monitor our press releases and check our website regularly until
the Annual Meeting for updated information.
We are holding the Annual Meeting for the following purposes, which
are more fully described in the accompanying proxy statement:
1. To
elect Ajit S. Shetty as a Class III director to serve for
a three-year term that expires at the
2025 Annual Meeting of Stockholders, or until his successor is
elected and qualified or until his earlier resignation or
removal;
2. To
approve an amendment to the Actinium Pharmaceuticals’ Inc. 2019
Plan to increase the total number of shares of common stock
authorized for issuance under such plan from 5,833,333 by
3,500,000, to a total of 9,333,333 shares to attract and retain the
best available personnel and to support planned hiring efforts as
the Company grows;
3. To
ratify the appointment of Marcum LLP as our independent registered
public accounting firm for the fiscal year ending December 31,
2022; and
4. To
approve, on a non-binding advisory
basis, the compensation of our named executive officers.
In addition, stockholders may be asked to consider and vote upon
such other business as may properly come before the Annual Meeting
or any adjournment or postponement thereof. After careful
consideration, the Board of Directors
unanimously recommends a vote “FOR” Proposals 1,
2, 3
and 4.
Only stockholders of record as of November 14, 2022 (the
“Record Date”) are entitled to notice of, and to vote at, the
Annual Meeting and any postponement or adjournment thereof. For ten
calendar days prior to the Annual Meeting, a complete list of
the stockholders entitled to vote at the Annual Meeting will be
available during ordinary business hours at our principal
executive offices for examination by any stockholder for any
purpose relating to the Annual Meeting. If you want to inspect the
stockholder list prior to the meeting, please contact us by
e-mail to
investorrelations@actiniumpharma.com or by mail to Actinium
Pharmaceuticals, Inc., 275 Madison Avenue, 7th Floor,
New York, New York 10016. The email should state the
purpose of the request and provide proof of ownership of our voting
securities as of the Record Date. Such list of the stockholders
will also be available during the Annual Meeting.
Your vote as an Actinium Pharmaceutical, Inc. stockholder is very
important. With respect to all matters that will come before the
Annual Meeting, each holder of shares of common stock is entitled
to one vote for each share of common stock held as of the Record
Date. For questions regarding your stock ownership, if you are a
registered holder, you can contact our transfer agent, Action Stock
Transfer by phone at (801) 274-1088.
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If your shares are
registered in your name, even if you plan to attend the
Annual Meeting or any postponement or adjournment of the Annual
Meeting in person, we request that you vote via the Internet, by
telephone, or by signing, dating and returning the enclosed proxy
card to ensure that your shares will be represented at the Annual
Meeting.
If your shares are held in
the name of a broker, trust, bank or other nominee, and you
receive these materials through your broker or through another
intermediary, please complete and return the materials in
accordance with the instructions provided to you by such broker or
other intermediary or contact your broker directly in order to
obtain a proxy issued to you by your nominee holder to attend the
Annual Meeting and vote in person. Failure to do so may result in
your shares not being eligible to be voted by proxy at the Annual
Meeting.
|
|
By Order of our Board of Directors,
|
|
|
/s/ Sandesh Seth
|
|
|
Chairman and Chief
Executive Officer
|
New York, NY
|
|
|
November 21, 2022
|
|
|
Table of
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TABLE OF
CONTENTS
Stockholders Should Read the
Entire Proxy Statement Carefully Prior to Submitting Their
Proxies
i
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PROXY
STATEMENT
FOR
ANNUAL MEETING
OF STOCKHOLDERS
GENERAL
Unless the context otherwise requires, references in this proxy
statement to “we,” “us,” “our,” “the Company,” or “Actinium” refer
to Actinium Pharmaceuticals, Inc., a Delaware corporation, and its
subsidiaries as a whole. In addition, unless the context otherwise
requires, references to “stockholders” are to the holders of our
common stock, par value $0.001 per share.
The enclosed proxy is solicited on behalf of the Board of Directors
of Actinium Pharmaceuticals, Inc. (the “Board”) for use at our 2022
annual meeting of stockholders of the Company (the “Annual
Meeting”) to be held on December 8, 2022, at the time and
place and for the purposes set forth in the accompanying Notice of
Annual Meeting of Stockholders and at any adjournment(s) or
postponement(s) of the Annual Meeting. Voting materials,
including this proxy statement and proxy card, are dated November
21, 2022 and are expected to be first made available to
stockholders on or about November 21, 2022.
The executive offices of the Company are located at, and the
mailing address of the Company is 275 Madison Avenue, 7th Floor,
New York, New York 10016.
IMPORTANT NOTICE REGARDING
THE AVAILABILITY OF PROXY MATERIALS
FOR THE STOCKHOLDER
MEETING TO BE HELD ON
December 8, 2022:
This proxy statement, a form of the proxy card and our 2021 annual
report to stockholders on Form 10-K (the “Annual Report”) are available for
viewing, printing and downloading at http://www.viewproxy.com/actiniumpharma/2022
or by email at: requests@viewproxy.com.
To view these materials, please have your control number available
that appears on your proxy card. On this website, you can also
elect to receive future distributions of our proxy statements and
annual reports to stockholders by electronic delivery.
Additionally, you can find a copy of our Annual Report, which
includes our financial statements at www.sec.gov, or in
the “SEC Filings” section of the “Investors” section of our website
at www.actiniumpharma.com.
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QuESTIONS
AND ANSWERS
Following are some commonly asked questions raised by our
stockholders and answers to each of those questions.
What is a proxy?
A proxy is another person that you legally designate to vote your
stock. If you designate someone as your proxy in a written
document, that document is also called a “proxy” or a “proxy card.”
If you are a “street name” holder, you must obtain a proxy from
your broker or nominee in order to vote your shares in person at
the Annual Meeting.
What is a proxy
statement?
A proxy statement is a document that regulations of the SEC require
that we give to you when we ask you to sign a proxy card to vote
your shares at the Annual Meeting.
What may I vote on at
the annual meeting?
At the Annual Meeting, stockholders will consider and vote upon the
following matters:
Proposal 1: To
elect Ajit S. Shetty as a Class III director to serve for
a three-year term that expires at the
2025 Annual Meeting of Stockholders, or until his successor is
elected and qualified or until his earlier resignation or
removal;
Proposal 2: To
approve an amendment to the Actinium Pharmaceuticals’ Inc. 2019
Plan to increase the total number of shares of common stock
authorized for issuance under such plan from 5,833,333 by
3,500,000, to a total of 9,333,333 shares to attract and retain the
best available personnel and to support planned hiring efforts as
the Company grows; and
Proposal 3: To
ratify the appointment of Marcum LLP (“Marcum”) as our independent
registered public accounting firm for the fiscal year ending
December 31, 2022.
Proposal 4: To
approve, on a non-binding advisory
basis, the compensation of our named executive officers.
To consider and act upon any other business as may properly come
before the Annual Meeting or any postponement or adjournment
thereof.
How does the Board recommend
that I vote on the proposals?
Our Board unanimously recommends that the stockholders vote “FOR”
Proposals 1, 2, 3 and 4 being put before our stockholders at the
Annual Meeting.
What should I do
if I receive more than one set of voting materials?
You may receive more than one set of the proxy materials
(consisting of this proxy statement, the accompanying Notice, our
2021 Annual Report and the proxy card) or voting instruction card.
For example, if you hold your shares in more than one brokerage
account, you will receive a separate voting instruction card for
each brokerage account in which you hold shares. Similarly, if you
are a stockholder of record and also hold shares in a brokerage
account, you will receive a copy of the proxy materials, including
a proxy card, for shares held in your name and a voting instruction
card for shares held in “street name.” Please complete, sign, date
and return each proxy card and voting instruction card that you
receive to ensure that all of your shares are voted.
What is the record date and
what does it mean?
The record date to determine the stockholders entitled to notice of
and to vote at the Annual Meeting is the close of business on
November 14, 2022 (the “Record Date”). The Record Date is
established by the Board as required by Delaware law. On the Record
Date, 25,483,306 shares of common stock were issued and
outstanding.
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Who is entitled to vote at
the Annual Meeting?
Holders of common stock at the close of business on the Record Date
may vote at the Annual Meeting.
What are the voting rights of
the stockholders?
Each holder of common stock is entitled to one vote per share of
common stock on each matter to be acted upon at the Annual Meeting.
Our Certificate of Incorporation, as amended (the “Charter”) does
not provide for cumulative voting rights.
What happens if a change to
the Annual Meeting is necessary due to exigent
circumstances?
While as of the date of this proxy statement we are intending to
hold the Annual Meeting in a physical format, as part of our
precautions regarding the COVID-19, we
reserve the right to reconsider the date, time, and/or means of
convening the Annual Meeting, including holding the Annual Meeting
by means of remote communications. If we take this step, we will
announce the decision to do so as soon as practicable via a press
release that will also be filed with the SEC as proxy material, as
well as by posting details on our website at https://www.actiniumpharma.com/. Please
monitor our press releases and check our website regularly until
the Annual Meeting for updated information.
What is the difference
between a stockholder of record and a “street name”
holder?
If your shares are registered directly in your name with Action
Stock Transfer Corporation, the Company’s stock transfer agent, you
are considered the stockholder of record with respect to those
shares. The Notice of Annual Meeting and the accompanying proxy
materials have been sent directly to you by the Company.
If your shares are held in a stock brokerage account or by a bank
or other nominee, the nominee is considered the record holder of
those shares. You are considered the beneficial owner of these
shares, and your shares are held in “street name.” The Notice of
Annual Meeting and the accompanying proxy materials would have been
forwarded to you by your nominee. As the beneficial owner, you have
the right to direct your nominee concerning how to vote your shares
by using the voting instructions the nominee included in the
mailing or by following such nominee’s instructions for voting.
What is a broker
non-vote?
Broker non-votes occur when shares are
held indirectly through a broker, bank or other intermediary on
behalf of a beneficial owner (referred to as held in “street name”)
and the broker submits a proxy but does not vote for a matter
because the broker has not received voting instructions from the
beneficial owner and either (i) the broker does not have
discretionary voting authority on the matter or (ii) the
broker chooses not to vote on a matter for which it has
discretionary voting authority. Under the rules of the
New York Stock Exchange that govern how brokers may vote
shares for which they have not received voting instructions from
the beneficial owner, brokers are permitted to exercise
discretionary voting authority only on “routine” matters when
voting instructions have not been timely received from a beneficial
owner. Proposal 3 is considered a “routine matter.” Therefore,
if you do not provide voting instructions to your broker regarding
such proposal, your broker will be permitted to exercise
discretionary voting authority to vote your shares on such
proposal. In the absence of specific instructions from you, your
broker does not have discretionary authority to vote your shares
with respect to Proposals 1, 2, and 4.
How do I
vote?
If you are a record holder, you may vote your shares at the Annual
Meeting in person or by proxy. Whether you plan to attend the
Annual Meeting or not, we urge you to vote by proxy. If you vote by
proxy, the individuals named on the proxy card, or your “proxies,”
will vote your shares in the manner you indicate. You may specify
whether your shares should be voted for or withheld for the
nominees for director or should be voted for, against or abstained
with respect to the amendment of the 2019 Plan and the ratification
of the appointment of the Company’s independent
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registered public accountants. Voting by proxy will not affect your
right to attend the Annual Meeting. If your shares are registered
directly in your name through our transfer agent, Action Stock
Transfer Corporation, or you have stock certificates registered in
your name, you may submit a proxy to vote:
• By Internet or by
telephone. Stockholders may vote via
the Internet at www.AALvote.com/atnm
or by phone (as per instructions on the proxy card). You will need
the control number included on your proxy card.
• By
mail. If you received one or more
printed proxy cards by mail, you can vote by mail by completing,
signing, dating and returning the enclosed proxy card applicable to
your class of stock in the enclosed postage prepaid envelope. Your
proxy will be voted in accordance with your instructions. If you
sign the proxy card but do not specify how you want your shares
voted, they will be voted as recommended by our Board.
• In person at the
Annual Meeting. If you attend the
Annual Meeting, you may deliver your completed proxy card in person
or you may vote by completing a ballot, which will be available at
the Annual Meeting. You are required to register in advance of the
Annual Meeting if you plan to attend the Annual Meeting in person.
If you wish to register in advance of the Annual Meeting, please
contact our investor relations office by no later than
November 28, 2022, by
e-mail to investorrelations@actiniumpharma.com,
mail to Actinium Pharmaceuticals, Inc., 275 Madison Avenue,
7th Floor,
New York, New York 10016, or telephone at
(646) 677-3875.
Telephone and Internet voting facilities for all stockholders of
record will be available 24-hours
a day and will close at 11:59 p.m., Eastern Standard
Time, on December 7, 2022.
The proxy is fairly simple to complete, with specific instructions
on the electronic ballot, telephone or proxy card. By completing
and submitting it, you will direct the proxies to vote your shares
at the Annual Meeting in accordance with your instructions. The
Board has appointed Sandesh Seth to serve as the proxy for the
Annual Meeting.
If your shares are held in “street name” (held in the name of a
bank, broker or other nominee who is the holder of record), you
must provide the bank, broker or other nominee with instructions on
how to vote your shares and can do so as follows:
• By Internet or by
telephone. Follow the instructions
you receive from the record holder to vote by Internet or
telephone.
• By
mail. You should receive instructions
from the record holder explaining how to vote your shares.
• In person at the
Annual Meeting. Contact the broker,
bank or other nominee who holds your shares to obtain a broker’s
proxy card and bring it with you to the Annual Meeting. You will
not be able to vote at the Annual Meeting unless you have a proxy
card from your broker, bank or other nominee.
What happens if additional
matters are presented at the Annual Meeting?
Other than the election of directors, the amendment of our 2019
Plan, the ratification of the appointment of our auditor and the
advisory vote on the compensation of our named executive officers,
we are not aware of any other business to be acted upon at the
annual meeting. If you grant a proxy, the person named as proxy
holder, Sandesh Seth, our Chairman and Chief Executive Officer
will have the discretion to vote your shares on any additional
matters properly presented for a vote at the Annual Meeting.
What happens if I do not
give specific voting instructions?
If you hold shares in your name and you sign and return a proxy
card without giving specific voting instructions, your shares will
be voted as recommended by our Board on all matters and as the
proxy holder may determine in his discretion with respect to any
other matters properly presented for a vote before the Annual
Meeting. If you hold your shares through a stockbroker, bank or
other nominee and you do not provide instructions on how to vote,
your stockbroker or other nominee may exercise their discretionary
voting power with respect to certain
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proposals that are considered as “routine” matters. Proposal 3
— ratification of the appointment of Marcum as our independent
registered public accounting firm is considered a routine matter,
and thus your stockbroker, bank or other nominee may exercise their
discretionary voting power with respect to Proposal 3.
If
the organization that holds your shares does not receive
instructions from you on how to vote your shares on a
non-routine
matter, the organization that
holds your shares will inform us that it does not have the
authority to vote on these matters with respect to your
shares. This is generally referred to as a “broker
non-vote.” In the absence of specific
instructions from you, your broker does not have discretionary
authority to vote your shares with respect to Proposal 1
— the election of Ajit S. Shetty as a member to our
Board, Proposal 2 — the approval of the amendment to the
2019 Plan, and Proposal 4 — the advisory vote on the
compensation of our named executive officers. We encourage you to
provide voting instructions to the organization that holds your
shares by carefully following the instructions provided in the
notice.
What is the quorum
requirement for the annual meeting?
On November 14, 2022, the Record Date for determining which
stockholders are entitled to vote, there were 25,483,306 shares of
our common stock outstanding, which is our only class of voting
securities. Each share of common stock entitles the holder to one
vote on matters submitted to a vote of our stockholders.
Thirty-Four percent (34%) of our
outstanding shares of common stock as of the Record Date must be
present at the Annual Meeting (in person or represented by proxy)
in order to hold the Annual Meeting and conduct business. This is
called a quorum. Your shares will be counted for purposes of
determining if there is a quorum, even if you wish to abstain from
voting on some or all matters introduced at the Annual Meeting, if
you are present and vote in person at the Annual Meeting or have
properly submitted a proxy card or voted by fax, by phone or by
using the Internet. Broker non-votes
will be counted for purposes of determining whether a quorum is
present.
Who counts the
votes?
All votes will be tabulated by Gary Siegel, our Vice President,
Controller, the inspector of election appointed for the Annual
Meeting. Each proposal will be tabulated separately.
How can I change my vote
after I return my proxy card?
You may revoke your proxy and change your vote at any time before
the final vote at the Annual Meeting. You may do this by signing a
new proxy card with a later date, by voting on a later date by
using the Internet (only your latest Internet proxy submitted prior
to the Annual Meeting will be counted), or by attending the Annual
Meeting and voting in person. However, your attendance at the
Annual Meeting will not automatically revoke your proxy unless you
vote at the Annual Meeting or submit a notice of revocation to the
Company addressed to Steve O’Loughlin, at the Company’s
address above, which notice must be received before 5:00 p.m.,
Eastern Time, on November 28, 2022.
Is my vote
confidential?
Proxy instructions, ballots and voting tabulations that identify
individual stockholders are handled in a manner that protects your
voting privacy. Your vote will not be disclosed either within our
company or to third parties, except:
• as
necessary to meet applicable legal requirements;
• to
allow for the tabulation of votes and certification of the vote;
and
• to
facilitate a successful proxy solicitation.
Any written comments that a stockholder might include on the proxy
card will be forwarded to our management.
Where can I find the
voting results of the Annual Meeting?
The preliminary voting results will be announced at the Annual
Meeting. The final voting results will be tallied by our Inspector
of Elections and reported in a Current Report on
Form 8-K which we will file with
the SEC, within four business days of the date of the Annual
Meeting.
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How can I obtain a
separate set of voting materials?
To reduce the expense of delivering duplicate voting materials to
our stockholders who may have more than one Actinium
Pharmaceuticals, Inc. stock account, we are delivering only one
proxy statement to certain stockholders who share an address,
unless otherwise requested. This practice, known as “householding.”
If you share an address with another stockholder and have received
only one proxy statement, you may write or call us to request to
receive a separate proxy statement. Similarly, if you share an
address with another stockholder and have received multiple copies
of the proxy statement, you may write or call us at the address and
phone number below to request delivery of a single copy of the
proxy statement. For future annual meetings of stockholders, you
may request separate proxy statements, or request that we send only
one proxy statement to you if you are receiving multiple copies, by
writing or calling us at:
Actinium Pharmaceuticals, Inc.
Attention: Steve O’Loughlin, Chief Financial Officer
275 Madison Avenue, 7th Floor
New York, New York 10016
Tel: (646) 677-3875
Stockholders who own shares through a bank, broker or other
intermediary can request householding by contacting the
intermediary.
We hereby undertake to deliver promptly, upon written or oral
request, a copy of the proxy statement to a stockholder at a shared
address to which a single copy of the document was delivered.
Requests should be directed to the address or phone number set
forth above.
Who pays for the cost of this
proxy solicitation?
Our Board is asking for your proxy, and we will pay the costs of
the solicitation of proxies. We may also reimburse brokerage firms
and other persons representing beneficial owners of shares for
expenses incurred in forwarding the voting materials to their
customers who are beneficial owners and obtaining their voting
instructions. In addition to soliciting proxies by mail, our Board
members, officers and employees may solicit proxies on our behalf,
without additional compensation, personally, electronically or by
telephone. In addition, we have retained Alliance Advisors, LLC
(“Alliance”) to assist in the solicitation of proxies for a fee of
$10,000 plus customary expenses.
Is this proxy statement the
only way that proxies are being solicited?
No. In addition to the solicitation of proxies by use of the mail,
officers and employees of the Company, as well as Alliance, the
proxy solicitation firm hired by the Company, may solicit the
return of proxies, either by mail, telephone, telecopy,
e-mail or through personal contact.
These officers and employees will not receive additional
compensation for their efforts but will be reimbursed for
out-of-pocket expenses. The fees of Alliance as well as
the reimbursement of expenses of Alliance will be borne by the
Company. Brokerage houses and other custodians, nominees and
fiduciaries, in connection with shares of the common stock
registered in their names, will be requested to forward
solicitation material to the beneficial owners of shares of common
stock.
How can I obtain a copy
of Actinium Pharmaceuticals, Inc.’s Annual Report?
This proxy statement and the Annual Report are available for
viewing, printing and downloading at www.viewproxy.com/actiniumpharma/2022. To view
these materials, please have your 11-digit control number(s) available that
appears on your proxy card. On this website, you can also elect to
receive future distributions of our proxy statements and annual
reports to stockholders by electronic delivery.
Additionally, you can find a copy of our Annual Report, which
includes our financial statements, for the fiscal year ended
December 31, 2021 on the website of the SEC, at www.sec.gov, or in
the “All SEC Filings” section of the “Investors” section of our
website at www.actiniumpharma.com.
You may also obtain a printed copy of our Annual Report, including
our financial statements, free of charge, from us by sending a
written request to: Actinium Pharmaceuticals, Inc., 275 Madison
Avenue, 7th Floor,
New York, NY 10016, attention: Chief Financial
Officer.
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What is the voting
requirement to elect directors?
Assuming the presence of a quorum, directors are elected by a
plurality of the votes cast in person or by proxy at the
Annual Meeting and entitled to vote on the election of directors.
“Plurality” means that the nominees receiving the greatest number
of affirmative votes will be elected as directors, up to the number
of directors to be chosen at the Annual Meeting. Abstentions or
broker non-votes will not affect the
outcome of the election of directors.
What is the voting
requirement to approve Proposal 2?
Assuming the presence of a quorum, the proposal to approve the
amendment to the 2019 Plan will require approval by a majority of
votes cast, with abstentions counting as a vote cast. An abstention
is not an “affirmative vote,” but it is considered as a vote cast
pursuant to Section 711 of the NYSE American Company Guide.
Accordingly, an abstention will have the effect of a vote against
Proposal 2. Broker non-votes will
have no effect on Proposal 2.
What is the voting
requirement to approve Proposal 3?
Assuming the presence of a quorum, the proposal to ratify the
appointment of Marcum as our independent registered public
accounting firm will be approved if the affirmative vote of a
majority of the shares represented in person or by proxy and
entitled to vote thereon at the Annual Meeting is obtained. An
abstention is not an “affirmative vote,” but an abstaining
stockholder is considered “entitled to vote” at the Annual Meeting.
Accordingly, an abstention will have the effect of a vote against
Proposal 3. Brokers are considered “entitled to vote” because
brokers have discretionary voting authority on Proposal 3.
Because a broker non-vote is not an
“affirmative vote,” a broker non-vote
will have the effect of a vote against Proposal 3.
What is the voting
requirement to approve Proposal 4?
Assuming the presence of a quorum, the advisory vote on the
compensation of our named executive officers will be approved if
the affirmative vote of a majority of the shares represented in
person or by proxy and entitled to vote thereon at the Annual
Meeting is obtained. An abstention is not an “affirmative vote,”
but an abstaining stockholder is considered “entitled to vote” at
the Annual Meeting. Accordingly, an abstention will have the effect
of a vote against Proposal 4. Broker non-votes will have no effect on Proposal 4.
Do I Have Dissenters’
(Appraisal) Rights?
Appraisal rights are not available to our stockholders with any of
the proposals described above to be brought before the Annual
Meeting.
How can I communicate
with the non-employee
directors on the Actinium
Pharmaceuticals, Inc. Board of Directors?
Our Board encourages stockholders who are interested in
communicating directly with the non-employee directors as a group to do so by writing
to the non-employee directors in care
of our Chairman and Chief Executive Officer. Stockholders can send
communications by mail to:
Sandesh Seth, Chairman and Chief Executive Officer
Actinium Pharmaceuticals, Inc.
275 Madison Avenue, 7th Floor
New York, New York 10016
Correspondence received that is addressed to the non-employee directors will be reviewed by our
Chairman of the Board or his designee, who will regularly forward
to the non-employee directors a
summary of all such correspondence and copies of all correspondence
that, in the opinion of our Chairman, deals with the functions of
our Board or committees thereof or that our Chairman otherwise
determines requires their attention. Directors may at any time
review a log of all correspondence received by us that is addressed
to the non-employee members of our
Board and request copies of any such correspondence.
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WHO
CAN HELP ANSWER YOUR QUESTIONS?
You may seek answers to your questions by writing, calling or
emailing us at:
Steve O’Loughlin
Chief Financial Officer
Actinium Pharmaceuticals, Inc.
275 Madison Avenue, 7th Floor
New York, NY 10016
Email: soloughlin@actiniumpharma.com
Tel: 646-677-3875
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CORPORATE
GOVERNANCE
Board of Directors
The Board oversees our business affairs and monitors the
performance of management. In accordance with our corporate
governance principles, our Board does not involve itself
in day-to-day operations. The directors keep themselves
informed through discussions with the Chairman and Chief Executive
Officer, other key executives, and by reading the reports and other
materials that we send them and by participating in Board and
committee meetings. Biographical information about our directors is
provided in the section “Directors and Executive Officers”.
Term of Office
Our directors are divided into three classes, designated
Class I, Class II and Class III. Class I
consists of two directors, Class II consists of two directors,
and Class III consists of one director.
The term of each director is set forth below or until their
successors are duly elected:
Director
|
|
Class
|
|
Term Expiration
|
David Nicholson
|
|
Class I
|
|
2023 Annual Meeting
|
Richard I Steinhart
|
|
Class I
|
|
2023 Annual Meeting
|
Sandesh Seth
|
|
Class II
|
|
2024 Annual Meeting
|
Jeffrey W. Chell
|
|
Class II
|
|
2024 Annual Meeting
|
Ajit S. Shetty
|
|
Class III
|
|
2022 Annual Meeting
|
Directors elected at each annual meeting are elected for a
three-year term. Notwithstanding the
foregoing, each director shall serve until his successor is duly
elected and qualified, or until his retirement, death, resignation
or removal.
Director
Independence
We use the definition of “independence” of the NYSE American stock
exchange to make this determination. We are listed on the NYSE
American under the symbol “ATNM”. NYSE American corporate
governance rule Section 803(A)(2) provides that an
“independent director” means a person other than an executive
officer or employee of the company. No director qualifies as
independent unless the issuer’s board of directors affirmatively
determines that the director does not have a relationship that
would interfere with the exercise of independent judgment in
carrying out the responsibilities of a director. Under the NYSE
American director independence rules, Jeffrey W. Chell, David
Nicholson, Ajit S. Shetty, and Richard I. Steinhart
are independent directors of the Company.
Board Leadership Structure
and Role in Risk Oversight
Our Board currently consists of five directors, and the positions
of Chairman of the Board and principal executive officer are filled
by Mr. Sandesh Seth, coupled with a lead independent director
position to further strengthen the leadership structure. The Board
acknowledges that there are different leadership structures that
could allow it to effectively oversee the management of the risks
relating to the Company’s operations. However, our Board believes
that having Mr. Seth as the Chairman of the Board and the
Chief Executive Officer provides an efficient and effective
leadership model for the Company, as such structure allows our
independent directors to share responsibility in leading the Board,
while allowing Mr. Seth to focus primarily on managing the
operations of Company.
David Nicholson has been serving as our lead independent director
(the “Lead Independent Director”) since September 2017. Our
Lead Independent Director chairs the executive sessions of our
Board meetings; provides feedback to the Chairman and Chief
Executive Officer; if appropriate, and in coordination with
executive management, is available for consultation and direct
communication with major stockholders; and leads the Board’s
evaluation of the Chairman and Chief Executive Officer. We have a
separate chair for each committee of our Board, all of whom are
independent directors. The chairs of each committee report on the
activities of their committees in fulfilling their responsibilities
at the meetings of our Board.
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Our Board is responsible for overseeing the Company’s risk
management processes. The Board receives reports from management
concerning the Company’s assessment of risks and considers the
Company’s risk profile. The Board focus on the most significant
risks facing the Company and the Company’s general risk management
strategy. In addition, as part of its oversight of our Company’s
executive compensation program, the Board considers the impact of
such program, and the incentives created by the compensation awards
that it administers, on our Company’s risk profile. In addition,
the Board, based on the Compensation Committee’s review of all of
our compensation policies and procedures, considers the incentives
that they create and factors that may reduce the likelihood of
excessive risk taking and determines whether they present a
significant risk to our Company. The Board has determined that, for
all employees, our compensation programs do not encourage excessive
risk and instead encourage behaviors that support sustainable value
creation.
Board of Directors Meetings
and Attendance
During 2021, our Board held fourteen meetings. Each director
attended all of the meetings of our Board and of any committees of
which he was a member during the year ended December 31, 2021.
It is our policy that directors should make every effort to attend
the annual meeting of stockholders. At our 2021 Annual Meeting of
stockholders, the Company was represented by our Chief Financial
Officer and Vice President, Controller with our Chairman and CEO
participating by phone and no other directors in attendance as no
shareholders registered to attend in advance of the meeting.
Code
of Business Conduct and Ethics
We adopted a Code of Business Conduct and Ethics that applies to
all of our directors, officers and employees, including our
principal executive officer and principal financial and accounting
officer. The Code of Business Conduct and Ethics addresses, among
other things, competition and fair dealing, conflicts of interest,
protection and proper use of Company assets, government relations,
compliance with laws, rules and regulations and the process for
reporting violations of the Code of Business Conduct and Ethics,
employee misconduct, improper conflicts of interest or other
violations. A copy of the Code of Business Conduct and Ethics is
available on the Investor section of our website at www.actiniumpharma.com.
We will post on our website any amendment to our Code of Business
Conduct and Ethics or waivers of our Code of Business Conduct and
Ethics for directors and executive officers.
Under our Code of Business Conduct and Ethics, no Corporate
director, officer or other employee, agent or contractor may,
directly or indirectly, sell any equity security, including
derivatives, of the Corporation (1) if he or she does not own
the security sold, or (2) if he or she owns the security, does
not deliver it against such sale (a “short sale against the box”)
within twenty days thereafter, or does not within
five days after such sale deposit it in the mails or other
usual channels of transportation. No Corporate director, officer or
other employee, agent or contractor may engage in short sales,
which are defined as any transactions whereby one may benefit from
a decline in the Corporation’s stock price.
Complaints Regarding
Accounting Matters
The Audit Committee has established procedures for:
• the
receipt, retention and treatment of complaints regarding
accounting, internal accounting controls, or auditing matters;
and
• the
confidential, anonymous submission by our employees of concerns
regarding questionable accounting or auditing matters.
Communications with
Directors
The Board has approved procedures for stockholders to send
communications to individual directors or the non-employee directors as a group. Written
correspondence should be addressed to the director or directors in
care of Sandesh Seth, Chairman and Chief Executive Officer of
Actinium Pharmaceuticals, Inc., 275 Madison Avenue, 7th Floor,
New York, NY 10016. Correspondence received that is
addressed to the non-employee
directors will be reviewed by our Chairman and Chief Executive
Officer or his designee, who will regularly forward to the
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non-employee directors a summary of
all such correspondence and copies of all correspondence that,
deals with the functions of our Board or committees thereof or that
he otherwise determines requires their attention. Directors may at
any time review a log of all correspondence received by us that is
addressed to the non-employee members
of our Board and request copies of any such correspondence. You may
also contact individual directors by calling our principal
executive offices at (646) 677-3875.
Legal Proceedings
There have been no material legal proceedings that would require
disclosure under the federal securities laws that are material to
an evaluation of the ability or integrity of our directors or
executive officers, or in which any director, officer, nominee or
principal stockholder, or any affiliate thereof, is a party adverse
to us or has a material interest adverse to us.
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BOARD
COMMITTEES
Committees of the Board of
Directors
Our Board has formed three standing committees: Audit, Compensation
and Nominating and Corporate Governance. Actions taken by our
committees are reported to the full Board. Each of our committees
has a charter and each charter is posted on our website.
Audit Committee
|
|
Compensation
Committee
|
|
Nominating and
Corporate Governance Committee
|
Richard I. Steinhart*
|
|
David Nicholson*
|
|
Ajit S. Shetty*
|
Jeffrey W. Chell
|
|
Jeffrey W. Chell
|
|
David Nicholson
|
Ajit S. Shetty
|
|
Ajit S. Shetty
|
|
Richard I. Steinhart
|
Audit Committee
Our Audit Committee, which currently consists of three directors,
provides assistance to our Board in fulfilling its legal and
fiduciary obligations with respect to matters involving the
accounting, financial reporting, internal control and compliance
functions of the Company. The Board has determined that
Mr. Steinhart is an “audit committee financial expert” as
defined in Item 407(d)(5)(ii) of
Regulation S-K. Our Audit
Committee employs an independent registered public accounting firm
to audit the financial statements of the Company and perform other
assigned duties. Further, our Audit Committee provides general
oversight with respect to the accounting principles employed in
financial reporting and the adequacy of our internal controls. In
discharging its responsibilities, our Audit Committee may rely on
the reports, findings and representations of the Company’s
auditors, legal counsel, and responsible officers. Our Board has
determined that all members of the Audit Committee are financially
literate within the meaning of SEC rules and under the current
listing standards of the NYSE American. The Audit Committee met
four times during 2021. Each member of the Audit Committee was
present at all of the Audit Committee meetings held during such
director’s tenure as a member of the Audit Committee.
Compensation
Committee
Our Compensation Committee, which currently consists of three
directors, establishes executive compensation policies consistent
with the Company’s objectives and stockholder interests. The
Compensation Committee met three times during 2021. Each member of
the Compensation Committee was present at the meeting held in 2021.
Our Compensation Committee also reviews the performance of our
executive officers and establishes, adjusts and awards
compensation, including incentive-based compensation, as more fully discussed
below. In addition, our Compensation Committee generally is
responsible for:
• establishing
and periodically reviewing our compensation philosophy and the
adequacy of compensation plans and programs for our directors,
executive officers and other employees;
• overseeing
our compensation plans, including the establishment of performance
goals under the Company’s incentive compensation arrangements and
the review of performance against those goals in determining
incentive award payouts;
• overseeing
our executive employment contracts, special retirement benefits,
severance, change in control arrangements and/or similar plans;
• acting
as administrator of any company stock option plans; and
• overseeing
outside compensation consultants when engaged.
Our Compensation Committee periodically reviews the compensation
paid to our non-employee directors and
the principles upon which their compensation is determined. The
Compensation Committee also periodically reports to the Board on
how our non-employee director
compensation practices compare with those of other similarly
situated public corporations and, if the Compensation Committee
deems it appropriate, recommends changes to our director
compensation practices to our Board for approval.
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Outside consulting firms retained by our compensation committee and
management also will, if requested, provide assistance to the
Compensation Committee in making its compensation-related decisions. The Compensation Committee
paid consultant fees to StreeterWyatt of $22,000 during the year
ended December 31, 2021. Streeter Wyatt was instructed to
providing support and analyses to the compensation committee and
their services included development of a peer group regarding
executive and director compensation.
Nominating and Corporate
Governance Committee
Our Nominating and Corporate Governance Committee, which currently
consists of three directors, is charged with the responsibility of
reviewing our corporate governance policies and proposing potential
director nominees to the Board for consideration. Our Board has
determined that each member of our Nominating and Corporate
Governance Committee qualifies as an “independent” member of the
Board as defined by the rules and regulations of the SEC and the
NYSE American. The Nominating and Corporate Governance Committee
was formed on November 4, 2021 and met one time during
2021.
Our Nominating and Corporate Governance Committee’s primary
responsibilities and obligations include, among other things:
• overseeing
the administration of our Code of Business Ethics and Conduct and
related policies;
• leading
the search for and recommending individuals qualified to become
members of the Board, and selecting director nominees to be
presented for election by the shareholders at each annual
meeting;
• ensuring,
in cooperation with the Compensation Committee, that no agreements
or arrangements are made with directors or relatives of directors
for providing professional or consulting services to us or our
affiliate or individual officer or one of their affiliated, without
appropriate review and evaluation for conflicts of interest;
• assessing
the independence of directors annually and report to the Board;
• recommending
to the Board for its approval, the leadership structure of the
Board, including whether the Board should have an executive or
non-executive Chairman, whether the
roles of Chairman and Chief Executive Officer should be combined,
and whether a Lead Director of the Board should be appointed;
provided that such structure shall be subject to the bylaws of the
Company then in effect;
• ensuring
that Board members do not serve on more than six other
for-profit public company boards that
have a class of securities registered under the Exchange Act
in addition to the Board;
• reviewing
the Board’s committee structure and to recommend to the Board for
its approval directors to serve as members of each committee as
well as recommendations for committee chairs;
• reviewing
and recommending changes to procedures whereby shareholders may
communicate with the Board;
• reviewing
recommendations received from shareholders for persons to be
considered for nomination to the Board;
• monitoring
compliance with our corporate governance guidelines;
• developing
and implementing an annual self-evaluation of the Board, both individually and as
a Board, and of its committees;
Our Nominating and Corporate Governance Committee considers all
qualified candidates identified by members of the Board, by senior
management and by stockholders. The Committee follows the same
process and uses the same criteria for evaluating candidates
proposed by stockholders, members of the Board and members of
senior management. When evaluating a candidate to serve on our
Board, the members of our Nominating and Corporate Governance
Committee consider items such as experience in the biotechnology
sector, experience with public companies, executive managerial
experience, operations and commercial experience, fundraising
experience and contacts in the investment banking industry,
personal and skill set compatibility with current Board members,
industry reputation, knowledge of our company generally, and
independence.
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Our Amended and Restated Bylaws, as amended (the “Bylaws”) contains
provisions that address the process by which a stockholder may
nominate an individual to stand for election to the Board at our
annual meetings. To recommend a nominee for election to the Board,
a stockholder must submit his or her recommendation to our
Secretary at our corporate offices at 275 Madison Avenue,
7th Floor,
New York, New York 10016. Such nomination must satisfy
the notice, information and consent requirements set forth in our
Bylaws and must be received by us prior to the date set forth under
“Submission of Future Stockholder Proposals” below. A stockholder’s
recommendation must be accompanied by the information with respect
to stockholder nominees as specified in our Bylaws, including among
other things, the name, age, address and occupation of the
recommended person, the proposing stockholder’s name and address,
the ownership interests of the proposing stockholder and any
beneficial owner on whose behalf the nomination is being made
(including the number of shares beneficially owned, any hedging,
derivative, short or other economic interests and any rights to
vote any shares) and any material monetary or other relationships
between the recommended person and the proposing stockholder and/or
the beneficial owners, if any, on whose behalf the nomination is
being made.
Our approach toward Board diversity takes into consideration the
overall composition and diversity of the Board and areas of
expertise that director nominees may be able to offer, including
business experience, knowledge, abilities, customer relationships
and appropriate perspectives on environmental, social and
governance matters. Generally, we strive to assemble and maintain a
Board that brings to us a variety of perspectives and skills
derived from business and professional experience as we may deem
are in our and our stockholders’ best interests. In doing so, we
also consider candidates with appropriate non-business backgrounds.
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DIRECTOR
COMPENSATION
The following table sets forth the compensation of our
non-employee directors for 2021:
Name
|
|
Fees
Earned or Paid in
Cash
|
|
Stock
Awards
|
|
Option Awards(1)
|
|
All Other Compensation
|
|
Total
|
Jeffrey W. Chell(2)
|
|
$
|
51,000
|
|
—
|
|
$
|
76,338
|
|
—
|
|
$
|
127,338
|
David Nicholson
|
|
$
|
63,000
|
|
—
|
|
$
|
76,338
|
|
—
|
|
$
|
139,338
|
Ajit S. Shetty
|
|
$
|
58,500
|
|
—
|
|
$
|
76,338
|
|
—
|
|
$
|
134,838
|
Richard Steinhart
|
|
$
|
63,000
|
|
—
|
|
$
|
76,338
|
|
—
|
|
$
|
139,338
|
Our non-employee directors are paid an
annual fee of $40,000 and receive annual option grants.
Dr. Nicholson as Lead Director receives an additional annual
fee of $10,000. Board committee members receive the following
compensation:
Board Committee
|
|
Chairman
|
|
Member
|
Audit
|
|
$
|
20,000
|
|
$
|
6,000
|
Compensation
|
|
$
|
10,000
|
|
$
|
5,000
|
Nominating and Corporate Governance
|
|
$
|
7,500
|
|
$
|
3,000
|
In 2021, we granted each non-employee
director options to purchase 18,351 shares of our common stock with
an exercise price of $6.07 per share with a term of 10 years.
Pursuant to the terms of the 2019 Plan, 2% of the options vest each
month from the date of grant.
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AUDIT
COMMITTEE REPORT
Report of the Audit Committee
of the Board of Directors
The Audit Committee provides assistance to the Board in fulfilling
its oversight responsibilities relating to our corporate accounting
and reporting practices toward assurance of the quality and
integrity of our consolidated financial statements. The purpose of
the Audit Committee is to serve as an independent and objective
party to monitor our financial reporting process and internal
control system; oversee, review and appraise the audit activities
of our independent registered public accounting firm and internal
auditing function, maintain complete, objective and open
communication between the Board, the independent accountants,
financial management and the internal audit function.
Our independent registered public accounting firm reports directly
to the Audit Committee, and the Audit Committee is solely
responsible to appoint or replace our independent registered public
accounting firm and to assure its independence and to provide
oversight and supervision thereof. The Audit Committee determines
compensation of the independent registered public accounting firm
and has established a policy for approval of non-audit related engagements awarded to the
independent registered public accounting firm. Such engagements
must not impair the independence of the registered public
accounting firm with respect to our Company as prescribed by the
Sarbanes — Oxley Act of 2002; thus payment
amounts are limited and non-audit
related engagements must be approved in advance by the Audit
Committee. The Audit Committee determines the extent of funding
that we must provide to the Audit Committee to carry out its duties
and has determined that such amounts were sufficient in 2021.
With respect to the fiscal year ended December 31, 2021, in
addition to its other work, the Audit Committee:
• Reviewed
and discussed with management our audited consolidated financial
statements as of December 31,
2021 and for the year then ended;
• Discussed
with Marcum the matters required to be discussed by the applicable
requirements of the Public Company Accounting Oversight Board
(“PCAOB”) and the SEC; and
• Received
the written disclosures and the letter from Marcum required by the
applicable requirements of the PCAOB regarding the independent
accountant’s communications with the Audit Committee concerning
independence and has discussed with Marcum its independence.
The Audit Committee recommended, based on the review and discussion
summarized above, that the Board include the 2021 audited
consolidated financial statements in the 2021
Form 10-K for the fiscal
year ended December 31, 2021 for filing with the SEC.
|
|
Audit Committee of the Board of Directors of
Actinium Pharmaceuticals, Inc.
|
|
|
|
|
|
|
|
|
|
Richard I. Steinhart, Chairman
Jeffrey W. Chell
Ajit S. Shetty
|
Information About Our
Auditors
Our Audit Committee of our Board appointed Marcum as the
independent registered public accounting firm to conduct the audit
of our consolidated financial statements for the 2021 fiscal year
and to report on our consolidated balance sheets, statements of
income and other related statements.
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Fees
and Services
The table below shows the aggregate fees billed for professional
services for the audits and audit-related fees of the Company’s annual financial
statements included in Form 10-K
for the years ending December 31, 2021 and 2020,
respectively, by Marcum LLP (PCAOB ID Number 688).
|
|
Year Ended December 31,
2021
|
|
Year Ended December 31,
2020
|
Audit Fees
|
|
$
|
128,400
|
|
$
|
130,004
|
Audit-Related Fees
|
|
|
20,600
|
|
|
83,630
|
Tax Fees
|
|
|
—
|
|
|
|
All Other Fees
|
|
|
—
|
|
|
|
Total
|
|
$
|
149,000
|
|
$
|
213,634
|
Audit Fees. This
category includes the audit of our annual consolidated financial
statements, reviews of our financial statements included in our
Form 10-Qs and services that are
normally provided by our independent registered public accounting
firm in connection with its engagements for those years.
Audit-Related
Fees. This
category consists of assurance and related services by our
independent registered public accounting firm that are reasonably
related to the performance of the audit or review of our financial
statements and are not reported above under “Audit Fees.” The
services for the fees disclosed under this category include
consents regarding equity issuances.
Pre-Approval
Policy
In 2015, the Audit Committee adopted policies and procedures for
the pre-approval of audit and
non-audit services performed by the
independent registered public accountants. Under the policies, the
Audit Committee is required to pre-approve all audit services and permitted
non-audit and tax services provided by
the independent registered public accountants in order to ensure
that the provision of such services does not impair the registered
accountants’ independence.
All of the services rendered by Marcum in 2021 were pre-approved by the Audit Committee.
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DIRECTORS
AND EXECUTIVE OFFICERS
Directors And Executive
Officers
The names, positions and ages of our directors and executive
officers as of November 14, 2022, are as follows:
Name
|
|
Age
|
|
Position
|
Sandesh Seth
|
|
58
|
|
Chairman and Chief Executive Officer
|
Steve O’Loughlin
|
|
37
|
|
Chief Financial Officer and Corporate Secretary (Principal
Financial and Accounting Officer)
|
Jeffrey W. Chell, M.D.
|
|
68
|
|
Director
|
David Nicholson, Ph.D.
|
|
67
|
|
Lead Independent Director
|
Richard I. Steinhart
|
|
65
|
|
Director
|
Ajit S. Shetty, Ph.D.
|
|
76
|
|
Director
|
Subject to the classified board provisions of our Charter, all
directors hold office until the next annual meeting of stockholders
and the election and qualification of their successors. Officers
are elected annually by the Board and serve at the discretion of
the Board.
There are no other arrangements or understanding between any of our
directors and any other persons pursuant to which they were
selected as a director.
Background of Executive
Officers and Directors
The principal occupations for the past five years (and, in
some instances, for prior years) of each of our directors and
executive officers are as follows:
Sandesh Seth, MS, MBA,
Chairman and Chief Executive Officer
Mr. Sandesh Seth has been our Chief Executive Officer since
June 2017. Mr. Seth has been a Director since
March 2012, our Chairman of the Board since October 2013,
and served as Executive Chairman from August 2014 to
June 2017.
Mr. Seth has 25+ years of experience in investment
banking (Laidlaw& Co (UK) Ltd., Cowen & Co.), equity
research (Bear Stearns, Commonwealth Associates) and in the pharma
industry (Pfizer, Warner-Lambert,
SmithKline in strategic planning, business development and R&D
project management). Mr. Seth was chairman of Relmada
Therapeutics Inc., a specialty pharma company focused on CNS
therapeutics, which he helped co-found. Mr. Seth has an MBA in Finance from
New York University; an M.S. in the Pharmaceutical Sciences
from the University of Oklahoma Health Center and a B.Sc. in
Chemistry from Bombay University. He has published several
scientific articles and was awarded the University Regents Award
for Research Excellence at the University of Oklahoma.
Mr. Seth was designated as Regulatory Affairs Certified by the
Regulatory Affairs Professionals Society which signifies
proficiency with U.S. FDA regulations. He has several patents
related to use of radiopharmaceuticals as conditioning agents for
adoptive cell therapies and as therapeutic combinations.
That Mr. Seth has served in various business
executive-level positions over the
course of his career, has significant investment banking
experience, has developed significant management, operational and
leadership skills and is well accustomed to interfacing with
investors, analysts, auditors, C-level
executives, and outside advisors, led us to conclude that
Mr. Seth should serve as a director.
Steve O’Loughlin, Chief
Financial Officer
Steve O’Loughlin has been our Chief Financial Officer since
August 2020. Mr. O’Loughlin served as our Principal
Financial Officer from May 2017 to August 2020.
Mr. O’Loughlin joined Actinium in October 2015 as Vice
President, Finance and Corporate Development, with almost a decade
of life sciences industry experience gained from previous positions
in investment banking and publicly traded life sciences companies.
Prior to Actinium, from June 2015 to October 2015,
Mr. O’Loughlin worked at J. Streicher LLC as an
investment banker, from August 2012 to June 2015
Mr. O’Loughlin held the position of vice president, corporate
finance and development and was a corporate officer at Protea
Biosciences, Inc., a publicly traded life sciences tools company.
Previously, From June 2010 to June 2012,
Mr. O’Loughlin held corporate development positions with
Caliber I.D., a publicly
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traded diagnostics company. Mr. O’Loughlin previously worked
in investment banking at Jesup & Lamont where he focused
on the biotechnology and life sciences industries.
Mr. O’Loughlin has a B.S. in Business Administration with a
concentration in finance from Ramapo College of New Jersey.
Jeffrey W. Chell, M.D.,
Director
Dr. Chell has been a Director of the Company since
April 2018. Dr. Chell is also a member of our Audit
Committee and Compensation Committee. He has been the chief
executive officer emeritus of the National Marrow Donor Program
(“NMDP”) since 2017 having served as its chief executive officer
since 2000. Dr. Chell has led the NMDP through
transformational growth as its Be The Match Registry tripled to
more than 12 million donors, the number of transplants
facilitated has grown fivefold to over 6,400 annually, and revenue
more than tripled to nearly $400 million per year. He is also
the co-founder and has served as
executive director of the Center For International Blood &
Marrow Transplant Research since 2004, a leading research program
in the field contributing over 70 research publications per year in
peer-reviewed journals. Dr. Chell
also currently serves as chair of CLR Insurance, a captive
insurance company domiciled in the Cayman Islands. From 2014 to
2016, Dr. Chell served as co-chair of Bone Marrow Donors Worldwide during its
IT transformation project, improving revenues and reducing
costs.
Prior to joining the NMDP, he served as president, Allina Medical
Clinics, a 450 physician multi-specialty medical group from 1994 to 1999. Prior
to that he practiced Internal Medicine in Minneapolis and in the
U.S. Air Force Medical Corps.
Dr. Chell received his M.D. from the University of Minnesota
and his training in Internal Medicine at the University of
Wisconsin, Madison. Dr. Chell is a diplomate of the American
Board of Internal Medicine, a member of the American Society of
Hematology and a member of the American Society of Blood and Marrow
Transplantation.
He has received multiple honors including the 2018 Public Service
award of the American Society For Blood and Marrow Transplantation,
2017 Most Admired CEO by the Minneapolis/St. Paul Business Journal,
2010 Healthcare Executive of the Year by the Minneapolis/St, Paul
Business Journal, and the 2017 Bone Marrow Foundation Service
Award.
That Dr. Chell brings many years of experience with
patient donor programs, knowledge of challenges related to bone
marrow transplants, leadership of organizations and experience
working in medical groups to our Board, led us to conclude that
Dr. Chell should serve as a director.
David Nicholson, Ph.D.,
Director
David Nicholson has been a Director of the Company since 2008.
Dr. Nicholson is also a member of our Compensation Committee
and our Nominating and Corporate Governance Committee. Since
March 2015, Dr. Nicholson served as Executive Vice
President and Chief R&D Officer of Allergan, which was acquired
by Abbvie in May 2020. In August 2014, Dr. Nicholson
joined Allergan (previously known as Actavis plc and Forest
Laboratories, Inc.) as senior vice president, Actavis Global Brands
R&D. From March 2012 to August 2014,
Dr. Nicholson was on the executive committee of Bayer
CropScience as head of research & development responsible
for the integration of the company’s R&D activities into one
global organization. Dr. Nicholson graduated in pharmacology,
earning his B.Sc. from the University of Manchester (1975) and
his Ph.D. from the University of Wales (1980). Between 1978 and
1988, Dr. Nicholson worked in the pharmaceutical industry for
the British company Beecham-Wülfing in Gronau,
Germany. The main emphasis of his activities as group leader in a
multidisciplinary project group was the development of
cardiovascular drugs.
From 1988-2007,
Dr. Nicholson held various positions of increasing seniority
in the UK, the Netherlands and the U.S. with Organon, a
business unit of Akzo Nobel. Ultimately, he became executive vice
president, research & development, and member of the
Organon Executive Management Committee. He implemented change
programs, leading to maximizing effectiveness in
research & development, ensuring customer focus and the
establishment of a competitive pipeline of innovative drugs. In
2007, Dr. Nicholson transferred to Schering-Plough, Kenilworth, New Jersey as senior vice
president, responsible for Global Project Management and Drug
Safety. From 2009 to December 2011, he was vice president
licensing and knowledge management at Merck in Rahway,
New Jersey, reporting to the president of Merck
R&D. As an integration team member, Dr. Nicholson
played a role in the strategic mergers of Organon BioSciences, the
human and animal health business of Dutch chemical giant
Akzo-Nobel, and Schering-Plough in 2007 as well as of Schering-Plough and Merck in 2009.
19
Table of
Contents
That Dr. Nicholson brings over 25 years of pharmaceutical
experience to our Board, having served in various pharmaceutical
research and development executive-level positions over the course of his career,
and that Dr. Nicholson has developed significant management
and leadership skills relating to the pharmaceutical industry and
is well accustomed to interfacing with investors, analysts,
auditors, outside advisors and governmental officials, led us to
conclude that Dr. Nicholson should serve as a director.
Ajit
S. Shetty, Ph.D., Director
Dr. Shetty has been a Director of the Company since
March 2017. Dr. Shetty is also a member of our Audit
Committee, Compensation Committee, and Chairman of our Nominating
and Corporate Governance Committee. Dr. Shetty joined Janssen
Pharmaceutical, Inc. (“Janssen”) in 1976 ultimately rising to the
position of president in 1986 where he led the establishment of
Janssen’s business in the U.S. From 1999 to 2008 he was
managing director of Janssen, during this time the Janssen Group of
companies’ global sales grew from $1 billion to
$8 billion, and from 2004 until 2012 he was chairman of the
board of directors. In Dr. Shetty’s most recent role at
Johnson & Johnson he was head of Enterprise Supply Chain,
where he reported to the chief executive officer and was
responsible for the transformation and optimization of Johnson&
Johnson’s supply chain. Dr. Shetty earned a Ph.D. in
Metallurgy and B.A. Natural Sciences from Trinity College,
Cambridge University and a Master of Business Administration from
Carnegie Mellon University. Dr. Shetty has served as a member
of Agile Therapeutics, Inc.’s board of directors since
February 2016. In 2007, Dr. Shetty was bestowed the title
of Baron by King Albert II of Belgium for his exceptional
merits. He is a member of the Board of Trustees of Carnegie Mellon
University, serves on the Board of Governors for GS1 (Global
Standards) in Belgium and formerly served on the Corporate Advisory
Board of the John Hopkins Carey Business School. In 2016,
Dr. Shetty was named as chairperson of the Vlaams Instituut
voor Biotechnologie (VIB), a Belgium based life sciences research
institute focused on translating scientific results into
pharmaceutical, agricultural and industrial applications. In
addition, he was elected Manager of the Year in 2004 in Flanders
and received a Life-Time Achievement
Award in India in 2010. We believe Dr. Shetty’s qualifications
to sit on our Board include his extensive pharmaceutical experience
leading commercial and supply chain operations and his significant
education background.
That Dr. Shetty has more than 30 years of leadership and
executive experience in the pharmaceutical industry, that he has
significant supply chain knowledge and that he has experience
conducting business in the U.S. and Europe, led us to conclude
that Dr. Shetty should serve as a director.
Richard I. Steinhart,
Director
Mr. Steinhart has served as our Director and Chairman of the
Audit Committee since November 2013. Mr. Steinhart is
also a member of our Nominating and Corporate Governance Committee.
Since October 2017 Mr. Steinhart has been the senior vice
president and chief financial officer of BioXcel Therapeutics, Inc.
Since March 2014, Mr. Steinhart has been a member of the
board of directors of Atossa Genetics, Inc. where he is chairman of
the audit committee and a member of the compensation committee.
From October 2015 to April 2017, Mr. Steinhart was
vice president and chief financial officer at Remedy
Pharmaceuticals, a privately-held,
clinical stage pharmaceutical company. From January 2014
through September 2015 Mr. Steinhart worked as a
financial and strategic consultant to the biotechnology and medical
device industries. From April 2006 through December 2013,
Mr. Steinhart was employed by MELA Sciences, Inc., as its vice
president, finance and chief financial officer, treasurer and
secretary. In April 2012, Mr. Steinhart received a
promotion to senior vice president, finance and chief financial
officer. From May 1992 until joining MELA Sciences,
Mr. Steinhart was a managing director of Forest Street
Capital/SAE Ventures, a boutique investment banking, venture
capital, and management consulting firm focused on healthcare and
technology companies. Prior to Forest Street Capital/SAE Ventures,
he was vice president and chief financial officer of Emisphere
Technologies, Inc. Mr. Steinhart’s other experience includes
seven years at CW Group, Inc., a venture capital firm focused
on medical technology and biopharmaceutical companies, where he was
a general partner and chief financial officer. Mr. Steinhart
began his career at Price Waterhouse, now known as
PricewaterhouseCoopers. He holds BBA and MBA degrees from Pace
University and is a Certified Public Accountant (inactive).
That Mr. Steinhart brings more than 30 years of financial
experience to our Board, having served in various
executive-level financial positions
over the course of his career, and that Mr. Steinhart is a
certified public accountant, led us to conclude that
Mr. Steinhart should serve as a director and chair the Audit
Committee.
20
Table of
Contents
EXECUTIVE
COMPENSATION
The following discussion
provides compensation information pursuant to SEC rules and may
contain statements regarding future individual and Company
performance targets and goals. These
targets and goals are disclosed in the limited context of the
Company’s compensation programs and should not be understood to be
statements of management’s expectations or estimates of results or
other guidance. We specifically caution stockholders not to apply
these statements to other contexts.
The following table sets forth the names and positions of:
(i) each person who served as our principal executive officer
during the year ended December 31, 2021; (ii) our two
most highly compensated executive officers, other than our
principal executive officer, who was serving as an executive
officer, as determined in accordance with the rules and regulations
promulgated by the SEC, as of December 31, 2021, with
compensation of $100,000 or more, and (iii) two additional
individuals for whom disclosure would have been provided pursuant
to clause (ii) but for the fact that the individuals were not
serving as our executive officers at December 31, 2021
(collectively our “Named Executive Officers”):
Name
|
|
Position
|
Sandesh Seth
|
|
Chairman and Chief Executive Officer
|
Steve O’Loughlin
|
|
Chief Financial Officer
|
Mark Berger*
|
|
Former Chief Medical Officer
|
Dale Ludwig**
|
|
Former Chief Scientific and Technology Officer
|
Summary Compensation
Table
The following table provides information regarding the compensation
earned during the years ended December 31, 2021 and 2020
for our named executive officers.
Name/Position
|
|
Year
|
|
Salary
|
|
Bonus(1)
|
|
Option
Awards(2)
|
|
All Other
Compensation
|
|
Total
|
Sandesh Seth
|
|
2021
|
|
$
|
615,000
|
|
$
|
430,000
|
|
$
|
1,290,323
|
|
$
|
—
|
|
$
|
2,335,323
|
Chairman and Chief
Executive Officer
|
|
2020
|
|
$
|
578,191
|
|
$
|
315,000
|
|
$
|
938,537
|
|
$
|
—
|
|
$
|
1,831,728
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Steve O’Loughlin
|
|
2021
|
|
$
|
370,000
|
|
$
|
150,000
|
|
$
|
447,034
|
|
$
|
—
|
|
$
|
967,034
|
Chief Financial
Officer
|
|
2020
|
|
$
|
330,000
|
|
$
|
90,000
|
|
$
|
398,640
|
|
$
|
—
|
|
$
|
818,640
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Mark Berger(3)
|
|
2021
|
|
$
|
304,962
|
|
$
|
—
|
|
$
|
279,395
|
|
$
|
—
|
|
$
|
584,357
|
Former Chief Medical
Officer
|
|
2020
|
|
$
|
415,000
|
|
$
|
100,000
|
|
$
|
314,958
|
|
$
|
—
|
|
$
|
829,958
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Dale Ludwig(4)
|
|
2021
|
|
$
|
213,068
|
|
$
|
—
|
|
$
|
—
|
|
$
|
—
|
|
$
|
213,068
|
Former Chief Scientific and
Technology Officer
|
|
2020
|
|
$
|
375,000
|
|
$
|
105,000
|
|
$
|
337,453
|
|
$
|
—
|
|
$
|
817,453
|
On September 1, 2021, Mr. Seth was granted an option to
purchase 310,182 shares of common stock and Mr. O’Loughlin was
granted an option to purchase 107,463 shares of common stock. The
options have an exercise price of $6.07 per share and will expire
on September 1, 2031. Pursuant to the terms of the Company’s
Amended and Restated 2019 Stock Plan, 2% of the options will vest
each month from October 1, 2021 until fully vested.
21
Table of
Contents
Narrative Disclosure to
Summary Compensation Table
Chief Executive Officer
Compensation
On August 12, 2020, we and Mr. Seth entered into an
employment agreement whereby Mr. Seth will serve as Chairman
and Chief Executive Officer until February 24, 2024, unless
terminated earlier as set forth in the employment agreement.
Under the terms of the employment agreement, Mr. Seth is
entitled to (i) a base salary, which will be determined by the
Board and adjusted to be competitively aligned to a range between
the 25th and 75th percentile of the
relevant market data of chief executive officer positions of
similarly situated publicly companies, (ii) a performance
bonus with a target of 50% of his annual base salary as well as
other multipliers as determined by the Board and (iii) options
to purchase shares of common stock of the Company as the Board may
grant. For 2020, Mr. Seth’s annual base salary was set at
$578,191, and for 2021, his annual base salary was set at $615,000.
When and if granted, options will have an exercise price equal to
the closing price of the Company’s common stock on the date of the
approval, and 2% of the grant will vest each month from the grant
date until fully vested, in accordance with the 2013 Stock Plan and
2019 Plan. The options will expire 10 years from the grant
date, subject to Mr. Seth’s continuing service with the
Company. Mr. Seth also receives the standard benefits
available to other similarly situated employees.
If Mr. Seth’s employment as Chief Executive Officer or
Chairman is terminated due to death or disability, Mr. Seth
will be entitled to earned, but unpaid, salary, benefits and the
Pro-Rated Bonus (as defined herein)
for the year of termination. Upon termination of his employment for
Cause (as defined in the employment agreement), or his resignation
without Good Reason (as defined in the employment agreement),
Mr. Seth will receive any accrued and unpaid base salary, the
Pro-Rated Bonus and benefits through
the date of termination.
If we terminate Mr. Seth’s employment without Cause, or if
Mr. Seth resigns for Good Reason, Mr. Seth will be
entitled to (i) a single lump sum payment equal to the
24 months of his compensation, (ii) continued health
benefits for 24 months, (iii) immediate vesting of all
outstanding equity awards granted to Mr. Seth, and (iv) a
single lump sum payment equal to his annual bonus subject to the
achievement of the applicable goals, pro-rated based on the number of days in the
Company’s fiscal year through the date of termination (the
“Pro-Rated Bonus”).
In addition, if we terminate Mr. Seth’s employment without
Cause or if Mr. Seth resigns for Good Reason, or if we fail to
renew his position as Chief Executive Officer and Chairman on
February 21, 2024, in any case, within the 12-month period beginning on the date of a Change in
Control (as defined in the 2013 Stock Plan and 2019 Plan),
Mr. Seth will be entitled to (i) a single lump sum
payment equal to 30 months of his compensation,
(ii) continued health benefits for 30 months,
(iii) immediate vesting of all outstanding equity awards
granted to Mr. Seth, and (iv) a single lump sum payment
equal to the Pro-Rated Bonus.
Chief Financial
Officer/Principal
Financial Officer Compensation
On August 12, 2020, we entered into an employment agreement
with Mr. O’Loughlin, pursuant to which he serves as Chief
Financial Officer of the Company. Under the terms of the employment
agreement, Mr. O’Loughlin is entitled to (i) a base
salary, which shall be determined by the Board, (ii) a
performance bonus, which may be up to 30% of the annual base salary
based upon the achievement of certain objectives such as the Board
shall determine and (iii) options to purchase shares of common
stock of the Company as the Board may grant. For 2020,
Mr. O’Loughlin’s annual base salary was set at $330,000, and
for 2021, his annual base salary was set at $370,000.
When and if granted, options will have an exercise price equal to
the closing price of the Company’s common stock on the date of the
approval, and 2% of the grant will vest each month from the grant
date until fully vested, in accordance with the 2013 Stock Plan and
2019 Plan. The options will expire 10 years from the grant
date, subject to Mr. O’Loughlin’s continuing service with the
Company. Mr. Loughlin will also receive the standard benefits
available to other similarly situated employees.
In addition, if we terminate Mr. O’Loughlin’s employment
without Cause (as defined in the employment agreement) or if
Mr. O’Loughlin resigns for Good Reason (as defined in the
employment agreement), in either case, within the 12-month period beginning on the date of a Change in
Control, Mr. O’Loughlin will be entitled to (i) a single
lump sum payment equal to his annual base salary,
(ii) continued health benefits for 12 months, and
(iii) immediate vesting of all outstanding equity awards
granted to Mr. O’Loughlin.
22
Table of
Contents
Former Chief Medical
Officer Compensation
On September 24, 2021, Dr. Berger resigned as the Chief
Medical Officer
In December 2016, we and Dr. Mark S. Berger entered
into an agreement (the “2016 Berger Employment Agreement”), to
employ Dr. Berger as our Chief Medical Officer.
Pursuant to the 2016 Berger Employment Agreement, Dr. Berger
was entitled to the following compensation and benefits:
• Dr. Berger’s
annual base salary was $405,000 in 2019. Dr. Berger was also
entitled to a cash bonus in an amount to be determined by the Board
with a target of 30% of the base salary.
• Dr. Berger
was eligible to participate in the Company’s benefit plans that are
generally provided for executive employees.
• From
time to time, the Board granted him options to purchase shares of
common stock of the Company.
On August 12, 2020, we entered into a new employment agreement
with Dr. Berger, pursuant to which he served as Chief Medical
Officer of the Company. Under the terms of the employment
agreement, Dr. Berger was entitled to (i) a base salary,
which shall be determined by the Board, (ii) a performance
bonus, which may be up to 30% of the annual base salary based upon
the achievement of certain objectives such as the Board shall
determine and (iii) options to purchase shares of common stock
of the Company as the Board may grant. For 2020, Dr. Berger’s
annual base salary was set at $415,000. When and if granted, the
options would have an exercise price equal to the closing price of
the Company’s common stock on the date of the approval, and 2% of
the grant would vest each month from the grant date until fully
vested, in accordance with the 2013 Stock Plan and 2019 Plan, as
applicable. The options expire 10 years from the grant date,
subject to Dr. Berger’s continuing service with the Company.
Mr. Berger also received the standard benefits available to
other similarly situated employees.
Former Chief Scientific and
Technology Officer Compensation
On July 26, 2021, Mr. Ludwig resigned as the Company’s
Chief Scientific and Technology Officer.
We and Dr. Dale Ludwig, effective January 2018, entered
into an Offer Letter pursuant to which Dr. Ludwig served as
the Company’s Chief Scientific Officer (the “Offer Letter”).
Pursuant to the Offer Letter. Dr. Ludwig was entitled to the
following compensation and benefits:
• Dr. Ludwig’s
annual base salary was $334,750 in 2019, and Dr. Ludwig was
entitled to a cash bonus in an amount to be determined by the Board
with a target of 30% of the base salary.
• From
time to time, the Board granted him options to purchase shares of
common stock of the Company.
• Dr. Ludwig
was eligible to receive all standard benefits that Company
employees are eligible to receive.
On August 12, 2020, we entered into a new employment agreement
with Dr. Ludwig, pursuant to which he served as Chief
Scientific and Technology Officer of the Company until his
resignation. Under the terms of the employment agreement,
Dr. Ludwig was entitled to (i) a base salary, which was
determined by the Board, (ii) a performance bonus, which could
have been up to 30% of the annual base salary based upon the
achievement of certain objectives such as the Board shall have
determined and (iii) options to purchase shares of common
stock of the Company as the Board may grant. For 2020,
Dr. Ludwig’s annual base salary was set at $375,000. When and
if granted, the options would have an exercise price equal to the
closing price of the Company’s common stock on the date of the
approval, and 2% of the grant would vest each month from the grant
date until fully vested, in accordance with the 2013 Stock Plan and
2019 Plan, as applicable. The options would expire 10 years
from the grant date, subject to Mr. Ludwig’s continuing
service with the Company. Dr. Ludwig would also receive the
standard benefits available to other similarly situated
employees.
23
Table of
Contents
OUTSTANDING EQUITY AWARDS AT FISCAL
YEAR-END
— 2021
The following table sets forth all unexercised options that have
been awarded to our named executives by the Company that were
outstanding as of December 31, 2021.
|
|
Option
Awards
|
|
|
|
Stock
Awards
|
Name
(a)
|
|
Number
of
Securities
Underlying
Unexercised
Options
(#)
(Exercisable)
(b)
|
|
Number
of
Securities
Underlying
Unexercised
Options
(#)
(Unexercisable)
(c)
|
|
Equity
Incentive
Plan
Awards:
Number
of
Securities
Underlying
Unexercised
Unearned
Options
(#)
(d)
|
|
Option
Exercise
Price
($)
(e)
|
|
Option
Expiration
Date
(f)
|
|
Number
of
Shares
or
Units
of
Stock
That
Have
Not
Vested
(#)
(g)
|
|
Market
Value
of
Shares
or
Units
of
Stock
That
Have
Not
Vested
($)
(h)
|
|
Equity
Incentive
Plan
Awards:
Number
of
Unearned
Shares,
Units
or
Other
Rights
That
Have
Not
Vested
(#)
(i)
|
|
Equity
Incentive
Plan
Awards:
Market
or
Payout
Value
of
Unearned
Shares,
Units or
Other
Rights
That
Have
Not
Vested
($)
(j)
|
Sandesh
Seth
|
|
832
|
(1)
|
|
—
|
|
—
|
|
45.05
|
|
8/30/2022
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
832
|
(1)
|
|
—
|
|
—
|
|
45.05
|
|
12/19/2022
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
9,333
|
(1)
|
|
—
|
|
—
|
|
183.90
|
|
9/23/2024
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
5,000
|
(1)
|
|
—
|
|
—
|
|
107.40
|
|
2/15/2025
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
16,666
|
(1)
|
|
—
|
|
—
|
|
59.70
|
|
4/15/2026
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
24,998
|
(1)
|
|
—
|
|
—
|
|
41.70
|
|
3/14/2027
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
27,333
|
(2)
|
|
6,000
|
|
—
|
|
23.487
|
|
7/13/2028
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
29,000
|
(2)
|
|
21,000
|
|
—
|
|
6.96
|
|
7/12/2029
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
44,496
|
(2)
|
|
94,566
|
|
—
|
|
9.55
|
|
8/12/2030
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
18,610
|
(2)
|
|
291,572
|
|
—
|
|
6.07
|
|
9/01/2031
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Steve
O’Loughlin
|
|
3,333
|
(1)
|
|
—
|
|
—
|
|
53.70
|
|
9/28/2025
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
1,666
|
(1)
|
|
—
|
|
—
|
|
59.70
|
|
4/15/2026
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
3,333
|
(1)
|
|
—
|
|
—
|
|
41.70
|
|
3/14/2027
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
7,243
|
(2)
|
|
1,590
|
|
—
|
|
23.487
|
|
7/13/2028
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
7,733
|
(2)
|
|
5,600
|
|
—
|
|
6.96
|
|
7/12/2029
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
18,896
|
(2)
|
|
40,170
|
|
—
|
|
9.55
|
|
8/12/2030
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
6,447
|
(2)
|
|
101,016
|
|
—
|
|
6.07
|
|
9/01/2031
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
|
|
|
|
|
|
|
|
|
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
|
|
|
|
|
|
|
|
|
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Mark
Berger(3)
|
|
—
|
|
|
—
|
|
—
|
|
—
|
|
—
|
|
—
|
|
—
|
|
—
|
|
—
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Dale
Ludwig(4)
|
|
—
|
|
|
—
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